Canonical Allele Identifier: CA2476012549

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270739G= , CM000663.2:g.85270739G=	GRCh38
NC_000001.10:g.85736422G= , CM000663.1:g.85736422G=	GRCh37
NC_000001.9:g.85509010G=	NCBI36
NG_012216.1:g.12162C=
NG_012216.2:g.11166C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.225C=	ENSP00000480561.2:p.Asn75=
ENST00000620248.2:c.225C=	ENSP00000480561.2:p.Asn75=
ENST00000648566.1:c.225C= MANE Select	ENSP00000498104.1:p.Asn75=
ENST00000649434.1:n.291C=
ENST00000650582.1:n.756C=
ENST00000370580.5:c.225C=	ENSP00000359612.1:p.Asn75=
ENST00000620248.1:c.225C=	ENSP00000480561.1:p.Asn75=
NM_003921.4:c.225C=	NP_003912.1:p.Asn75=
XM_005271311.2:c.225C=	XP_005271368.1:p.Asn75=
XM_011542397.1:c.384C=	XP_011540699.1:p.Asn128=
XM_011542398.1:c.384C=	XP_011540700.1:p.Asn128=
XM_011542399.1:c.171C=	XP_011540701.1:p.Asn57=
NM_001320715.1:c.225C=	NP_001307644.1:p.Asn75=
NM_003921.5:c.225C= MANE Select	NP_003912.1:p.Asn75=
XM_011542397.3:c.384C=	XP_011540699.1:p.Asn128=
XM_011542398.2:c.384C=	XP_011540700.1:p.Asn128=
XM_011542399.2:c.171C=	XP_011540701.1:p.Asn57=
NM_001320715.2:c.225C=	NP_001307644.1:p.Asn75=